Canonical Allele Identifier: PA1139720486
Gene: DSG2 HGNC NCBI

Linked Data

ClinVar Variation Id: 927518
ClinVar RCV Id: RCV001190832
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001934.2:p.Ser202Tyr
CA402133683
NM_001943.5:c.605C>A